Department of Biological Sciences, University of Southern California, 3616 Trousdale Parkway, Los Angeles, CA 90089-0371, USA.
Microb Ecol. 2011 Aug;62(2):383-98. doi: 10.1007/s00248-011-9816-9. Epub 2011 Mar 4.
Changes in the structure and composition of a protistan community were characterized through the analysis of small-subunit ribosomal RNA gene (18S) sequences for a 3-day bottle incubation using a single sample collected in the western North Atlantic. Cloning and sequencing was used to investigate changes in perceived species richness and diversity as a consequence of environmental perturbation. The treatments included a control (unamended seawater), inorganic nutrient enrichment, and enrichment with a complex organic mixture. Five clone libraries were constructed and analyzed at the time of collection (t-0 h) and after 24 (t-24 h) and 72 (t-72 h) h for the control, and at t-72 h for the inorganic and organic enrichments, resulting in an analysis of 1,626 partial 18S rDNA sequences that clustered into 238 operational taxonomic units (OTUs). Analysis of the clone libraries revealed that protistan assemblages were highly dynamic and changed substantially at both the OTU level and higher taxonomic classifications during time frames consistent with many oceanographic methods used for measuring biological rates. Changes were most dramatic in enrichments, which yielded community compositions that were strongly dominated by one or a few taxa. Changes in community structure during incubation dramatically influenced estimates of species richness, which were substantially lower with longer incubation and especially with amendment, even though all incubated samples originated from the same aliquot of seawater. Containment and enrichment of the seawater sample led to the detection of otherwise undetected protistan taxa, suggesting that characterization of protistan diversity in a sample only at the time of collection could lead to an underrepresentation of unique taxa. Additionally, the rapid increase in the relative abundance of some members of the "rare biosphere" in our results implies an ecological importance of at least some of the taxa comprising the "rare biosphere."
通过对取自北大西洋西部的单一水样进行为期 3 天的瓶式培养,并分析小亚基核糖体 RNA 基因(18S)序列,研究了原生生物群落的结构和组成变化。克隆和测序用于调查由于环境扰动而导致的感知物种丰富度和多样性的变化。处理包括对照(未添加海水)、无机养分富集和复杂有机混合物的富集。在采集时(t-0 h)以及对照的 24 小时(t-24 h)和 72 小时(t-72 h)和无机和有机富集的 72 小时(t-72 h)时构建和分析了 5 个克隆文库,分析了 1626 个部分 18S rDNA 序列,这些序列聚类为 238 个操作分类单元(OTU)。克隆文库分析表明,原生生物群落具有高度动态性,在 OTU 水平和更高的分类分类水平上都发生了很大变化,这与许多用于测量生物速率的海洋学方法一致。在培养过程中,变化最为剧烈,在富集中群落组成发生了强烈变化,主要由一个或几个分类群主导。培养过程中群落结构的变化极大地影响了物种丰富度的估计值,即使所有培养的样品都来自相同的海水样本,随着培养时间的延长和特别是在添加物的情况下,物种丰富度的估计值会大大降低。海水样本的封存和富集导致了原本无法检测到的原生生物类群的检测,这表明仅在采集时对样本中的原生生物多样性进行特征描述可能会导致独特类群的代表性不足。此外,我们的结果中一些“稀有生物圈”成员的相对丰度的快速增加意味着至少一些构成“稀有生物圈”的类群具有生态重要性。